Evidence map›Paper›PMID 37885367›Full record

ArticlePharmacology research & perspectives2023

The role of plasma concentrations and drug characteristics of beta-blockers in fall risk of older persons.

K J Ploegmakers, E P van Poelgeest, L J Seppala, S C van Dijk, L C P G M de Groot, S Oliai Araghi, N M van Schoor, B Stricker, K M A Swart, A G Uitterlinden and 2 more

Open access · goldAbstract read
In one paragraph

Article in Pharmacology research & perspectives, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
3.6field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 5 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors at 6 institutions in 1 country.

K J PloegmakersAmsterdam UMC Location University of Amsterdam, Internal Medicine, Section of Geriatric Medicine, Amsterdam, The Netherlands.ORCID 0000-0002-5772-8057
E P van PoelgeestAmsterdam UMC Location University of Amsterdam, Internal Medicine, Section of Geriatric Medicine, Amsterdam, The Netherlands.
L J SeppalaAmsterdam UMC Location University of Amsterdam, Internal Medicine, Section of Geriatric Medicine, Amsterdam, The Netherlands.
S C van DijkDepartment of Geriatrics, Franciscus Gasthuis & Vlietland, Rotterdam, the Netherlands.
L C P G M de GrootDivision of Human Nutrition and Health, Wageningen University, Wageningen, the Netherlands.
S Oliai AraghiDepartment of Epidemiology, Erasmus University Medical Center, Rotterdam, the Netherlands.
N M van SchoorAmsterdam Public Health, Aging and Later Life, Amsterdam, The Netherlands.
B StrickerDepartment of Epidemiology, Erasmus University Medical Center, Rotterdam, the Netherlands.
K M A SwartAmsterdam UMC Location Vrije Universiteit Amsterdam General Practice, Amsterdam, The Netherlands.
A G UitterlindenDepartment of Epidemiology, Erasmus University Medical Center, Rotterdam, the Netherlands.
R A A MathôtAmsterdam UMC Location University of Amsterdam, Hospital Pharmacy-Clinical Pharmacology, Amsterdam, The Netherlands.
N van der VeldeAmsterdam UMC Location University of Amsterdam, Internal Medicine, Section of Geriatric Medicine, Amsterdam, The Netherlands.
Amsterdam Neuroscience · NLErasmus MC · NLAmsterdam University Medical Centers · NLGGD Amsterdam · NLSint Franciscus Gasthuis · NLWageningen University & Research · NL

Funding

ZonMw 6130.0031
6 · The paper itself

Abstract

Beta-blocker usage is inconsistently associated with increased fall risk in the literature. However, due to age-related changes and interindividual heterogeneity in pharmacokinetics and dynamics, it is difficult to predict which older adults are more at risk for falls. Therefore, we wanted to explore whether elevated plasma concentrations of selective and nonselective beta-blockers are associated with an increased risk of falls in older beta-blocker users. To answer our research question, we analyzed samples of selective (metoprolol, n = 316) and nonselective beta-blockers (sotalol, timolol, propranolol, and carvedilol, n = 179) users from the B-PROOF cohort. The associations between the beta-blocker concentration and time to first fall were assessed using Cox proportional hazard models. Change of concentration over time in relation to fall risk was assessed with logistic regression models. Models were adjusted for potential confounders. Our results showed that above the median concentration of metoprolol was associated with an increased fall risk (HR 1.55 [1.11-2.16], p = .01). No association was found for nonselective beta-blocker concentrations. Also, changes in concentration over time were not associated with increased fall risk. To conclude, metoprolol plasma concentrations were associated with an increased risk of falls in metoprolol users while no associations were found for nonselective beta-blockers users. This might be caused by a decreased β1-selectivity in high plasma concentrations. In the future, beta-blocker concentrations could potentially help clinicians estimate fall risk in older beta-blockers users and personalize treatment.

Indexed as

Adrenergic beta-AntagonistsMetoprololAgedAged, 80 and overCarvedilolHumansAdrenergic beta-AntagonistsCarvedilolMetoprololaccidental fallsadrenergic beta-antagonistsmetoprololrisk assessment

Identifiers

PMID37885367
PMCPMC10603288
OpenAlexW4387965588

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.